PLUS™

GUDID 03663136033310

Left sagittal bender

SPINEVISION

Orthopaedic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 03663136033310
• NIH Device Record Key: 82ced09c-9663-435c-9be0-e6230655a7b2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PLUS™
• Version Model Number: U1-A329
• Company DUNS: 390377518
• Company Name: SPINEVISION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com
• Phone: +33153332525
• Email: corp.quality@spinevision.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03663136033310 [Primary]

FDA Product Code

• KWQ: Appliance, Fixation, Spinal Intervertebral Body

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

[03663136033310]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-11-14
• Device Publish Date: 2018-09-04

On-Brand Devices [PLUS™]

• 03663136033310: Left sagittal bender
• 03663136033303: Right sagittal bender